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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

ANKRD11 · rs2965940

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−13, with 1 associations in the GWAS Catalog.

How this is scored

4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.

What the study found

Who was studied 394,642 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0122 lower (95% confidence interval 0.0088-0.0156); p = 1 × 10−13.

How common The T allele had a frequency of about 46% in the people studied.

Where it sits Chromosome 16, band 16q24.3 — in an intron of ANKRD11.

How common each version is

GT
Korean KRGDB
G 45.4% · T 54.6%
Korean Korea4K
G 43.9% · T 56.1%
Korean Korea1K
G 43.4% · T 56.6%
Japanese ToMMo
G 37.6% · T 62.4%
Vietnamese
G 33.6% · T 66.4%
World gnomAD
G 49.4% · T 50.6%
World 1000 Genomes
G 47.7% · T 52.3%
World TOPMed
G 48.7% · T 51.3%

The share of all copies of this position that are each version. Source: the population studies published in dbSNP (US NCBI); each row names its study.

What each result means

G/G No copy of the version the research linked to Mean platelet thrombocyte volume (UKB data field 30100). This is the starting point the study compared everyone against.
G/T One copy of the version the research linked to Mean platelet thrombocyte volume (UKB data field 30100). That is a smaller link than two copies.
T/T Two copies of the version the research linked to Mean platelet thrombocyte volume (UKB data field 30100). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Quoting this page

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Mean platelet thrombocyte volume (UKB data field 30100) (rs2965940). MyGeneLog™. https://www.mygenelog.com/variants/rs2965940

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